AVS 48352008

GUDID 07613327268133

UniLIF TRIAL

Stryker Corporation

Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial

• Primary Device ID: 07613327268133
• NIH Device Record Key: b9bec009-20a2-49a6-9f7b-841fb80e560b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AVS
• Version Model Number: 48352008
• Catalog Number: 48352008
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter
• Height: 8 Millimeter
• Angle: 0 degree
• Length: 20 Millimeter
• Width: 8 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327268133 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

[07613327268133]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-12-10
• Device Publish Date: 2019-12-02

On-Brand Devices [AVS]

• 07613327267945: PL GRAFT BLOCK
• 07613327267693: AL SPACER SUPPORT
• 07613327267624: AS SPACER SUPPORT
• 07613327122169: PL TRIAL INSTRUMENT INSERT
• 07613327121193: TL PEEK CONTAINER
• 07613327120950: WIDE IMPLANT TRAY
• 07613327120943: IMPLANT TRAY
• 07613327119572: LID LONG IMPLANT SIZES
• 07613327119558: WIDE IMPLANT TRAY
• 07613327119541: WIDE IMPLANT TRAY
• 07613327119527: PL PEEK IMPLANT CONTAINER
• 07613327119503: PL PEEK INSTRUMENT CONTAINER
• 07613327119480: INSTRUMENTBASE
• 07613327119473: PL PEEK CONTAINER
• 07613327119466: PL PEEK CONTAINER
• 07613327119428: AL PEEK CONTAINER
• 07613327119411: AS PEEK CONTAINER
• 07613327270556: SPACER TRIAL
• 07613327270518: SPACER TRIAL
• 07613327270471: SPACER TRIAL
• 07613327270457: SPACER TRIAL
• 07613327270440: SPACER TRIAL
• 07613327270433: SPACER TRIAL
• 07613327270426: SPACER TRIAL
• 07613327270419: SPACER TRIAL
• 07613327270402: SPACER TRIAL
• 07613327270372: SPACER TRIAL
• 07613327270358: SPACER TRIAL
• 07613327270334: SPACER TRIAL
• 07613327268546: UniLIF TRIAL
• 07613327268270: UniLIF TRIAL
• 07613327268263: UniLIF TRIAL
• 07613327268256: UniLIF TRIAL
• 07613327268249: UniLIF TRIAL
• 07613327268232: UniLIF TRIAL
• 07613327268225: UniLIF TRIAL
• 07613327268218: UniLIF TRIAL
• 07613327268201: UniLIF TRIAL
• 07613327268195: UniLIF TRIAL
• 07613327268188: UniLIF TRIAL
• 07613327268171: UniLIF TRIAL
• 07613327268164: UniLIF TRIAL
• 07613327268157: UniLIF TRIAL
• 07613327268140: UniLIF TRIAL
• 07613327268133: UniLIF TRIAL
• 07613327268126: UniLIF TRIAL
• 07613327268119: UniLIF TRIAL
• 07613327268102: UniLIF TRIAL
• 07613327268096: UniLIF TRIAL
• 07613327268089: UniLIF TRIAL